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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 385182Generated: October 29, 2026

Hydrochloric Acid → HCID 10943393, compound

https://huagongshe.com/reaction/385182

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantIodineHCID 807—
Reactant5-Aminosalicylic AcidHCID 4075—
ReactantCarbon DisulfideHCID 6348—
ReactantTriethylamineHCID 8471—
ReactantSodium SulfiteHCID 24437—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 10943393HCID 10943393100%

Reaction Steps

Carbon disulfide (0.26 mL, 4.4 mmol) was added to a mixture comprising 5-amino-2-hydroxybenzoic acid (0.23 g, 1.5 mmol), tetrahydrofuran (1.0 mL), water (1.0 mL) and triethylamine (0.51 mL, 3.6 mmol), followed by stirring at room temperature for 17 hours. The obtained reaction mixture was dropwise added to a tetrahydrofuran (1.0 mL) solution of iodine (0.41 g, 1.6 mmol) over a period of 5 minutes at 0° C., followed by stirring at 0° C. for further 2.5 hours. Thereafter, 1M hydrochloric acid (1.5 mL) and sodium sulfite (38 mg, 0.30 mmol) were added and mixed. Then, ethyl acetate (6 mL) was added, and the organic layer was separated and concentrated under reduced pressure to dryness. To the residue, ethyl acetate (6 mL) and water (1 mL) were added, and the organic layer was concentrated under reduced pressure to dryness to obtain 5-isothiocyanato-2-hydroxybenzoic acid as a gray solid (0.29 g, yield: 100%, HPLC purity: 97%, HPLC retention time: 4.3 min). LC-MS ES-194 (retention time: 4.4 min, condition 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367857B2
Source datasetuspto-grants-2013_02
ORD IDord-a2c295b4e13c46a1b7768c749f529b76
Source noteuspto-grants-2013_02